has material basis in autosomal genetic disease glucose transporter type 1 deficiency syndrome UMLS_CUI:C1847501 MIM:PS606777 DOID:0070560 MIM:PS606777 disease_ontology A glucose metabolism disease characterized by deficient glucose transport over the blood-brain barrier and reduced glucose availability in the central nervous system that has_material_basis_in mutation in the SLC2A1 gene on chromosome 1p34.2. MESH:C536830 GLUT1DS UMLS_CUI:C1847501 MESH:C536830 ICD10CM:E74.810 glucose metabolism disease autosomal inheritance